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DOI | 10.3389/fimmu.2022.781222 |
The Prognostic Value of FoxP3+Tumour-Infiltrating Lymphocytes in Rectal Cancer Depends on Immune Phenotypes Defined by CD8+Cytotoxic T Cell Density | |
Schnellhardt, Soeren; Hirneth, Johannes; Buettner-Herold, Maike; Daniel, Christoph; Haderlein, Marlen; Hartmann, Arndt; Fietkau, Rainer; Distel, Luitpold | |
通讯作者 | Distel, L (corresponding author),Friedrich Alexander Univ Erlangen Nurnberg, Univ Klinikum Erlangen, Dept Radiat Oncol, Erlangen, Germany. ; Distel, L (corresponding author),Comprehens Canc Ctr Erlangen Europa Metropolreg N, Erlangen, Germany. |
来源期刊 | FRONTIERS IN IMMUNOLOGY
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ISSN | 1664-3224 |
出版年 | 2022 |
卷号 | 13 |
英文摘要 | Tumour-infiltrating FoxP3+ regulatory T cells have been identified as both positive and negative prognostic factors in colorectal cancer (CRC) and rectal cancer (RC). In this study we investigated whether immune phenotypes, defined by CD8+ cytotoxic T cell density, may influence the prognostic association of FoxP3+ T cell densities in RC. Tissue microarrays from 154 rectal cancer resections were immunohistochemically double stained for CD8 and FoxP3. CD8+ and FoxP3+ cell densities were measured in the stromal and intraepithelial compartment. Stromal FoxP3+ cell densities were not associated with 10-year overall survival (OS). In the immune-desert phenotype, defined by very low stromal CD8+ cell density, a high density of stromal FoxP3+ T cells displayed a tendency towards an association with decreased 10-year OS (p = 0.179). In inflamed tumours, defined by high intraepithelial CD8+ T cell infiltration, the opposite was the case and high stromal FoxP3+ T cell densities were a positive prognostic factor (p = 0.048). Additionally, patients with an increased FoxP3/CD8 cell density ratio demonstrated a strong trend towards decreased 10-year OS (p = 0.066). These contrasting findings suggest functional heterogeneity within the group of FoxP3+ T cells. They are consistent with experimental studies which reported suppressive and non-suppressive populations of FoxP3+ T cells in CRC. Furthermore, our study demonstrates that CD8 immunohistochemistry may act as an instrument to identify tumours infiltrated by possibly functionally differing FoxP3+ T cell subtypes. |
英文关键词 | Foxp3 CD8 regulatory T cells rectal cancer tumour-infiltrating lymphocytes TILs immune phenotypes prognosis |
类型 | Article |
语种 | 英语 |
开放获取类型 | Green Submitted, Green Published, gold |
收录类别 | SCI-E |
WOS记录号 | WOS:000752083400001 |
WOS关键词 | NEOADJUVANT CHEMORADIOTHERAPY ; TUMOR INFILTRATION ; EXPRESSION ; SURVIVAL |
WOS类目 | Immunology |
WOS研究方向 | Immunology |
资源类型 | 期刊论文 |
条目标识符 | http://119.78.100.177/qdio/handle/2XILL650/376518 |
作者单位 | [Schnellhardt, Soeren; Hirneth, Johannes; Haderlein, Marlen; Fietkau, Rainer; Distel, Luitpold] Friedrich Alexander Univ Erlangen Nurnberg, Univ Klinikum Erlangen, Dept Radiat Oncol, Erlangen, Germany; [Schnellhardt, Soeren; Hirneth, Johannes; Buettner-Herold, Maike; Daniel, Christoph; Haderlein, Marlen; Hartmann, Arndt; Fietkau, Rainer; Distel, Luitpold] Comprehens Canc Ctr Erlangen Europa Metropolreg N, Erlangen, Germany; [Buettner-Herold, Maike; Daniel, Christoph] Friedrich Alexander Univ Erlangen Nurnberg, Univ Klinikum Erlangen, Dept Nephropathol, Inst Pathol, Erlangen, Germany; [Hartmann, Arndt] Friedrich Alexander Univ Erlangen Nurnberg, Univ Klinikum Erlangen, Inst Pathol, Erlangen, Germany |
推荐引用方式 GB/T 7714 | Schnellhardt, Soeren,Hirneth, Johannes,Buettner-Herold, Maike,et al. The Prognostic Value of FoxP3+Tumour-Infiltrating Lymphocytes in Rectal Cancer Depends on Immune Phenotypes Defined by CD8+Cytotoxic T Cell Density[J],2022,13. |
APA | Schnellhardt, Soeren.,Hirneth, Johannes.,Buettner-Herold, Maike.,Daniel, Christoph.,Haderlein, Marlen.,...&Distel, Luitpold.(2022).The Prognostic Value of FoxP3+Tumour-Infiltrating Lymphocytes in Rectal Cancer Depends on Immune Phenotypes Defined by CD8+Cytotoxic T Cell Density.FRONTIERS IN IMMUNOLOGY,13. |
MLA | Schnellhardt, Soeren,et al."The Prognostic Value of FoxP3+Tumour-Infiltrating Lymphocytes in Rectal Cancer Depends on Immune Phenotypes Defined by CD8+Cytotoxic T Cell Density".FRONTIERS IN IMMUNOLOGY 13(2022). |
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